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Sequence of the mouse adenovirus type-1 DNA encoding the 100-kDa, 33-kDa and DNA-binding proteins
Institution:1. Ambulatory Care Services, Denver Health, Denver, Colo;2. Department of Pediatrics, University of Colorado School of Medicine, Aurora, Colo;3. Institute for Health Research, Kaiser Permanente Colorado, Denver, Colo;4. Department of Internal Medicine, Massachusetts General Hospital, Boston, Mass;5. Genomic Medicine Institute Geisinger Health System, Danville, Pa;1. Área de Enfermedades del Corazón, Hospital Universitario de Bellvitge, IDIBELL, Universidad de Barcelona, L’Hospitalet de Llobregat, Barcelona, España;2. Subdirección de Gerencia, Hospital Universitario de Bellvitge, IDIBELL, Universidad de Barcelona, L’Hospitalet de Llobregat, Barcelona, España
Abstract:The genomic nucleotide sequence for the region of 66 to 77 map units (m.u.) of mouse adenovirus type 1 (MAV-1) was determined and predicted to encode proteins homologous to the human adenovirus (Ad) 100-kDa, 33-kDa and DNA-binding proteins (DBP). The putative MAV-1 100-kDa protein has 65-70% amino-acid similarity to 100-kDa proteins from five different human Ad serotypes. The mRNA for the putative 33-kDa protein is internally spliced within the coding sequence, as are its human Ad counterparts Oosterom-Dragon and Anderson, J. Virol. 45 (1983) 251–;263]. The N-terminal region of the putative MAV-1 33-kDa protein has 41–;44% similarity to two human Ad 33-kDa N-termini, and the C-terminal regions are more conserved, with 60–;65% similarity. The MAV-1 DBP is predicted to be encoded in this region and was compared to six different human Ad DBP N- and C-termini. The N-termini of the MAV-1 and Ad DBP were 33–48% similar and the C-termini were 56–60% similar. The MAV-1 DBP contains conserved regions (CR) 1, 2 and 3, and it retains important residues for a putative zinc finger (Zf) motif identified in Ad DBP Eagle and Klessig, Virology 187 (1992) 777–;787]. Additional sequence features of these three proteins have also been identified.
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